Exercise and myotonic dystrophy: A 31P magnetic resonance spectroscopy and magnetic resonance imaging case study [2]

Annals of Neurology

Volumn 59, Issue 5, 2006, Pages 871-872

  Trenell, Michael I ^a   Thompson, Campbell H ^b   Sue, Carolyn M ^a  

^a UNIVERSITY OF SYDNEY   (Australia)

^b FLINDERS UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE PHOSPHATE; PHOSPHATE; PHOSPHODIESTER; UNCLASSIFIED DRUG;

ADULT; AEROBIC EXERCISE; CASE REPORT; CONTROLLED STUDY; DMPK GENE; EXERCISE; GENE; HUMAN; LETTER; MALE; MUSCLE MASS; MUSCLE MITOCHONDRION; MYOTONIC DYSTROPHY; PHOSPHORUS NUCLEAR MAGNETIC RESONANCE; PRIORITY JOURNAL;

EXERCISE; EXERCISE THERAPY; HUMANS; MAGNETIC RESONANCE IMAGING; MAGNETIC RESONANCE SPECTROSCOPY; MALE; MIDDLE AGED; MYOTONIC DYSTROPHY;

EID: 33646360171     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20841     Document Type: Letter

References (4)

1. Ørngreen MC, Olsen DB, Vissing J. Aerobic training in patients with myotonic dystrophy type 1. Ann Neurol 2005;57:754-757.
2. Trenell MI, Sue CM, Sachinwalla T, et al. Aerobic exercise and muscle metabolism in patients with mitochondrial myopathy. Muscle Nerve 2006;33:524-531.
3. Kemp GJ, Taylor DJ, Dunn JF, et al. Cellular energetics of dystrophic muscle. J Neurol Sci 1993;116:201-206.
4. 31P magnetic resonance spectroscopy study. Brain 1997;120:1699-1711.